Human Phenotype Ontology 
Grandparent Node:
Abnormal oblique muscle physiology (HP:0031739)help
Parent Node:
Abnormal inferior oblique muscle physiology (HP:0025596)help
..Starting node
Inferior oblique muscle weakness (HP:0025598)help
Term ID: 25598
Name: Inferior oblique muscle weakness
Synonym: Inferior oblique palsy
Definition: Decreased strength of the inferior oblique muscle.
Reference: HP:0025598
Genes and Diseases:
       Child Nodes:
........expandInferior oblique muscle restriction (HP:0025597) help
........expandInferior oblique muscle underaction (HP:0031741) help

 Sister Nodes: 
..expandInferior oblique muscle overaction (HP:0025599) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025598HP:0025598Inferior oblique muscle weakness0 CL E G H
HP:0025598HP:0031741Inferior oblique muscle underaction1 CL E G H
HP:0025598HP:0025597Inferior oblique muscle restriction1 CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.